Abstract
The reaction of Co(NCS)2 with 4-methyl-pyridine N-oxide (C6H7NO) leads to the formation of two compounds, namely, tetra-kis-(4-methyl-pyridine N-oxide-κO)bis-(thio-cyanato-κN)cobalt(II), [Co(NCS)2(C6H7NO)4] (1), and tris-(4-methyl-pyridine N-oxide-κO)bis-(thio-cyanato-κN)cobalt(II), [Co(NCS)2(C6H7NO)3] (2). The asymmetric unit of 1 consists of one CoII cation located on a centre of inversion, as well as one thio-cyanate anion and two 4-methyl-pyridine N-oxide coligands in general positions. The CoII cations are octa-hedrally coordinated by two terminal N-bonding thio-cyanate anions in trans positions and four 4-methyl-pyridine N-oxide ligands. In the extended structure, these complexes are linked by C-H⋯O and C-H⋯S inter-actions. In compound 2, two crystallographically independent complexes are present, which occupy general positions. In each of these complexes, the CoII cations are coordinated in a trigonal-bipyramidal manner by two terminal N-bonding thio-cyanate anions in axial positions and by three 4-methyl-pyridine N-oxide ligands in equatorial positions. In the crystal, these complex mol-ecules are linked by C-H⋯S inter-actions. For compound 2, a nonmerohedral twin refinement was performed. Powder X-ray diffraction (PXRD) reveals that 2 was nearly obtained as a pure phase, which is not possible for compound 1. Differential thermoanalysis and thermogravimetry data (DTA-TG) show that compound 2 start to decompose at about 518 K.